PRR14
Proline-rich protein 14
Also known as: MGC3121, PRR14_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BWN1
- Gene
- PRR14
- Ensembl
- ENSG00000156858
- Chromosome
- 16
- Canonical length
- 585 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
The protein encoded by this gene tethers heterochromatin to the nuclear laminar scaffold by binding heterochromatin protein 1 (HP1) and the nuclear lamina. The tether is broken during mitosis and reforms quickly after mitosis, with the encoded protein first binding HP1 and then attaching to the nuclear lamina. This protein also has been shown to promote MyoD activity and skeletal myogenesis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Feb 2016]
Canonical amino-acid sequenceUniProt
585 residues, UniProt reviewed canonical sequence.
>Q9BWN1|PRR14
1 MDLPGDSSPP GQPRLCRQPL TRALWGARSP KRPRLQLPGA PSPLEKASRR VLAVVLEDVM
61 AVHMVPVVPS KQTSIPQHHS YHQDPVHRQP PASPPRQAGW SSQARPPDPL CLCREPLSRI
121 HRTSSTLRRR SRTTPGPEEG PSQKVDRAPQ PTLVVMLEDI ASPRPPAEGF IDETPNFIIP
181 AQRAEPMRIV RQPTPPPGDL EPPFQPSALP ADPLESPPTA PDPALELPST PPPSSLLRPR
241 LSPWGLAPLF RSVRSKLESF ADIFLTPNKT PQPPPPSPPM KLELKIAISE AEQSGAAEGT
301 ASVSPRPPIR QWRTQDHNTP ALLPKPSLGR SYSCPDLGPP GPGTCTWPPA PPQPSRPRPR
361 RHTVGGGEMA RAPPPPRPCL RKEVFPLGGV GASPSLTTSC SSTASTSFSE PAEPRLGSTK
421 GKEPRASKDQ VLSEPETKTM GKVSRFRIRR TPARPQLNLT PMGLPRPIRL NKKEFSLEEI
481 YTNKNYQSPT TRRTFETIFE EPRERNGTLI FTSSRKLRRA VEFRDSSLPR SRRPSRGVRA
541 AGGRTVPPNV APSPDVGPLL QQRLEELDAL LLEEETVDRE QPHWTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against PRR14 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.7
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- cerebellum: 38 nTPM
- spleen: 34 nTPM
- colon: 31 nTPM
- endometrium: 30 nTPM
- blood vessel: 29 nTPM
- cervix: 28 nTPM
Single-cell type
- neutrophils: 46 nCPM
- esophageal apical cells: 32 nCPM
- megakaryocytes: 31 nCPM
- esophageal basal cells: 30 nCPM
- epididymal efferent duct absorptive cells: 29 nCPM
- breast myoepithelial cells: 28 nCPM
Immune cell
- eosinophil: 24 nTPM
- neutrophil: 23 nTPM
- basophil: 11 nTPM
- non-classical monocyte: 11 nTPM
- naive B-cell: 11 nTPM
- T-reg: 10 nTPM
Brain region
- cerebral cortex: 28 nTPM
- cerebellum: 26 nTPM
- medulla oblongata: 25 nTPM
- thalamus: 24 nTPM
- white matter: 23 nTPM
- amygdala: 22 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.47
- gnomAD pLI
- 0.17
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of PRR14 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads PRR14 as an antibody target. Whether an autoantibody or antibody against PRR14 could matter depends on whether native PRR14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
PRR14 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label PRR14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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